VIVO Positioning Patches

Primary DI
00851424007102
Brand
VIVO Positioning Patches
Company
Catheter Precision, Inc.
Model
9208
Catalog number
9208
Device description
Patches are placed on the shoulder and sternum of the patient to acquire an image for VIVO analysis.
Published
2026-02-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
DQKComputer, Diagnostic, Programmable

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQKComputer, Diagnostic, ProgrammableCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K200313000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K200313000VIVOCatheter Precision, Inc.2020-09-14DQK

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00085142400710PackageGS15In Commercial Distribution
00851424007102PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00085142400710000851424007100851424007100085142400710
00851424007102008514240071028514240071020851424007102

GMDN Terms#

Term, Definition table
TermDefinition
Cardiac mapping system application software"An individual software program or group of programs, routines and/or algorithms that add specific image processing and/or analysis capabilities to a cardiac mapping system computer for storing, processing and management of electronic information/data used to interpret cardiac physiology parameters. It is a basic set of application programs and routines used for cardiac mapping computer-controlled imaging which can be upgraded to correct programming errors or to add new system capabilities. An application program package is typically identified by a proprietary name and ""version"" or ""upgrade"" number."

Regulatory Flags#

DUNS number
131845013
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00851424007089VIVO900290022026-02-03
00085142400710VIVO Positioning Patches920892082026-02-03
00851424007119VIVO System900290022026-02-03
00851424007140LockeT Suture Retention Devicev293012026-01-13
00851424007157LockeT Suture Retention Devicev293012026-01-13
00842362100017PharosEX-3082017-05-04
00842362100024DABRA Laser SystemRA-3082017-10-13
00842362100031DABRA 101 Catheter1012017-10-13

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Primary DI, Brand, Company table
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